Tyrosinemia: An inborn error of tyrosine metabolism with cirrhosis of the liver and multiple renal tubular defects (de Toni-Debré-Fanconi syndrome)
- 30 April 1965
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 66 (4), 670-696
- https://doi.org/10.1016/s0022-3476(65)80002-6
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- RENAL LESIONS IN WILSON'S DISEASEThe Lancet, 1964
- Delayed maturation of tyrosine metabolism in a full-term sibling of a child with phenylketonuriaThe Journal of Pediatrics, 1963
- Alternate pathways of p-hydroxyphenylacetic acid formation in the ratBiochimica et Biophysica Acta, 1961
- Turbidimetric Analysis of Inorganic Sulfate in Serum, Plasma and UrineScandinavian Journal of Clinical and Laboratory Investigation, 1960
- Some Investigations on the Metabolism of Phenylalanine and Tyrosine in Children with Vitamin C DeficiencyArchives of Disease in Childhood, 1957
- Multiple myeloma and the adult Fanconi syndrome: I. Report of a case with crystal-like deposits in the tumor cells and in the epithelial cells of the kidneyAmerican Journal Of Medicine, 1957
- CERTAIN ASPECTS OF TYROSINE METABOLISM IN THE YOUNG. I. THE DEVELOPMENT OF THE TYROSINE OXIDIZING SYSTEM IN HUMAN LIVER 1Journal of Clinical Investigation, 1956
- Experimental Production of Renal Glycosuria, Phosphaturia, and Aminoaciduria by Injection of Maleic AcidScience, 1954
- AMINO-ACIDURIA IN LEAD POISONING A CASE IN CHILDHOODThe Lancet, 1953
- Über Die Cystinkrankheit der Ersten LebenszeitKlinische Wochenschrift, 1937